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Cdmo Operations Manager Jobs (NOW HIRING)

Evergen

$100K - $120K/yr

Operations Manager Full-Time Alachua, FL, US Salary Range: $100,000.00 To $120,000.00 Annually ... CDMO) in regenerative medicine. As the only regenerative medicine company that offers a ...

Evergen

NY · On-site

$100K - $120K/yr

Operations Manager Full-Time Alachua, FL, US Salary Range: $100,000.00 To $120,000.00 Annually ... CDMO) in regenerative medicine. As the only regenerative medicine company that offers a ...

Evergen

Operations Manager

Alachua, FL · On-site

$100K - $120K/yr

... CDMO) in regenerative medicine. As the only regenerative medicine company that offers a ... Manages daily production meetings and understands relevant metrics and drivers in assigned ...

Eliassen Group

Supplier Operations Manager

Almont, CO · On-site

$75 - $85/hr

Manage coordination of Technical Operations contracts and purchase requisitions/purchase orders ... Potential future scope by mutual agreement: support CDMO vendor and site selection, ensure ...

kindeva

Metrology Manager

Saint Louis, MO

The Impact You Will Make The Manager of Metrology leads the site or multi-site calibration program supporting pharmaceutical CDMO manufacturing and laboratory operations. This role ensures ...

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Cdmo Operations Manager information

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How much do cdmo operations manager jobs pay per year?

As of Sep 10, 2026, the average yearly pay for cdmo operations manager in the United States is $63,456.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,000.00 and $77,500.00 per year, depending on experience, location, and employer.

What are popular job titles related to Cdmo Operations Manager jobs?

For Cdmo Operations Manager jobs, the most frequently searched job titles are:

Infographic showing various Cdmo Operations Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $63,456 per year, or $30.5 per hour.

Senior Scientist, Technology Transfer & CDMO Operations

San Diego, CA • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago

Job description

Summary
  • Lead end-to-end technology transfer and CDMO relationship management for radiopharmaceutical drug products, serving as the primary operational/technical liaison between internal teams and external CDMOs. Oversee the full CDMO lifecycle (selection/onboarding through clinical supply chain management) in alignment with Regulatory, Quality, and Clinical teams.
Responsibilities
  • Own technology transfer from internal development to domestic/international CDMOs (plans, timelines, success criteria).
  • Manage day-to-day CDMO relationships; resolve technical/operational issues; ensure quality, compliance, and delivery.
  • Oversee clinical supply chain (material flow, inventory, logistics, drug substance/product coordination).
  • Partner cross-functionally (Regulatory, Quality, Clinical) and communicate risks/status.
  • Lead agreements and documents (CDAs, Quality Agreements, Technical Packages, SOWs, supply agreements).
  • Develop technical transfer packages (process descriptions, batch records, analytical methods, specs, CMC documentation).
  • Support IND/CMC and quality activities (audits, gap assessments, CAPAs).
  • Maintain oversight through Phase 1+ (batch record reviews, deviations, change control, supply planning).
  • Support vendor qualification/RFP and due diligence.
  • Manage multiple concurrent projects (plans, risk registers, communication cadence).
  • Author and maintain program documentation; provide status reporting.
  • Travel up to 25–30%.
Education/Experience
  • BSc +7 years, MSc +5 years, or PhD +2 years in relevant scientific/engineering field with pharma/biopharma industry experience.
Preferred Qualifications
  • 5+ years direct tech transfer/CMC/manufacturing experience (pharma/biopharma/radiopharma).
  • Experience managing CDMOs across multiple geographies (ex-US strongly preferred).
  • IND-enabling and Phase 1 clinical manufacturing experience.
  • Radiopharmaceutical manufacturing/GMP familiarity.
  • Supply chain/clinical logistics experience preferred.
Skills/Qualifications
  • Working knowledge of CMC principles, GMP manufacturing, analytical method transfers, quality systems.
  • CDMO/vendor management; clinical supply chain knowledge (forecasting, logistics, cold chain, import/export considerations).
  • Document authoring (Quality Agreements, CDAs, Technical Packages, SOWs, regulatory CMC).
  • Strong project management (e.g., MS Project/Smartsheet; PMP a plus).
  • Cross-functional collaboration; clear written/verbal communication.
  • Regulatory awareness (FDA and international agencies).
  • Ethics/confidentiality; proactive problem-solving.
Benefits (if applicable)
  • Health coverage (medical/pharmacy/dental/vision), wellbeing programs, 401(k), disability/life insurance, and paid time off.
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